TEVA-HALOPERIDOL DIN 00363650
Health Canada record
| Active ingredient(s) | HALOPERIDOL 5 MG |
|---|---|
| Dosage form | Tablet |
| Route | Oral |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | N05AD01 HALOPERIDOL |
| Original market date | 31-Dec-1984 |
| Current status date | 12-Sep-2016 |
| Source | Health Canada DPD |
Establishment licence of the holder
Teva Canada Limited — licence 101810, currently licensed, last inspection rating C (2025-03-04).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing HALOPERIDOL
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 00808652 | HALOPERIDOL INJ 5MG/ML USP | SANDOZ CANADA INCORPORATED | Liquid | HALOPERIDOL 5 MG | Marketed |
| 02366010 | HALOPERIDOL INJECTION | JUNO PHARMA CANADA INC. | Solution | HALOPERIDOL 5 MG | Marketed |
| 02406411 | HALOPERIDOL INJECTION, USP | FRESENIUS KABI CANADA LTD | Solution | HALOPERIDOL 5 MG | Marketed |
| 00363685 | TEVA-HALOPERIDOL | TEVA CANADA LIMITED | Tablet | HALOPERIDOL 0.5 MG | Marketed |
| 00713449 | TEVA-HALOPERIDOL | TEVA CANADA LIMITED | Tablet | HALOPERIDOL 10 MG | Marketed |
| 00363669 | TEVA-HALOPERIDOL | TEVA CANADA LIMITED | Tablet | HALOPERIDOL 2 MG | Marketed |
| 00363677 | TEVA-HALOPERIDOL | TEVA CANADA LIMITED | Tablet | HALOPERIDOL 1 MG | Marketed |
| 00396818 | APO HALOPERIDOL TAB 1MG | APOTEX INC | Tablet | HALOPERIDOL 1 MG | Dormant |
| 00587702 | APO-HALOPERIDOL LIQ 2MG/ML | APOTEX INC | Solution | HALOPERIDOL 2 MG | Cancelled Post Market |
| 00463698 | APO-HALOPERIDOL TAB 10MG | APOTEX INC | Tablet | HALOPERIDOL 10 MG | Dormant |
| 00396826 | APO-HALOPERIDOL TAB 2MG | APOTEX INC | Tablet | HALOPERIDOL 2 MG | Dormant |
| 00396834 | APO-HALOPERIDOL TAB 5MG | APOTEX INC | Tablet | HALOPERIDOL 5 MG | Dormant |
| 00017574 | HALDOL INJECTION 5MG/ML | MCNEIL PHARMACEUTICAL, DIVISION OF ORTHO-MCNEIL INC. | Liquid | HALOPERIDOL 5 MG | Cancelled Post Market |
| 02540223 | HALOPERIDOL INJECTION | JUNO PHARMACEUTICALS CORP. | Solution | HALOPERIDOL 5 MG | Cancelled Pre Market |
| 02493993 | HALOPERIDOL INJECTION | NEO HEALTH CANADA INC. | Solution | HALOPERIDOL 5 MG | Cancelled (Unreturned Annual) |
| 00587788 | HALOPERIDOL TAB 1MG | PRO DOC LIMITEE | Tablet | HALOPERIDOL 1 MG | Cancelled Post Market |
| 00761745 | HALOPERIDOL TAB 2MG | PRO DOC LIMITEE | Tablet | HALOPERIDOL 2 MG | Cancelled Post Market |
| 00761753 | HALOPERIDOL TAB 5MG | PRO DOC LIMITEE | Tablet | HALOPERIDOL 5 MG | Cancelled Post Market |
| 00761761 | HALOPERIDOL-10 TAB 10MG | PRO DOC LIMITEE | Tablet | HALOPERIDOL 10 MG | Cancelled Post Market |
| 00745561 | NOVO-PERIDOL ORAL SOLN 2MG/ML | NOVOPHARM LIMITED | Solution | HALOPERIDOL 2 MG | Cancelled Post Market |
| 02239219 | NU-HALOPERIDOL | NU-PHARM INC | Tablet | HALOPERIDOL 5 MG | Cancelled (Unreturned Annual) |
| 02239217 | NU-HALOPERIDOL | NU-PHARM INC | Tablet | HALOPERIDOL 1 MG | Cancelled (Unreturned Annual) |
| 02239218 | NU-HALOPERIDOL | NU-PHARM INC | Tablet | HALOPERIDOL 2 MG | Cancelled (Unreturned Annual) |
| 02239220 | NU-HALOPERIDOL | NU-PHARM INC | Tablet | HALOPERIDOL 10 MG | Cancelled (Unreturned Annual) |
| 02239216 | NU-HALOPERIDOL | NU-PHARM INC | Tablet | HALOPERIDOL 0.5 MG | Cancelled (Unreturned Annual) |
| 00759503 | PMS-HALOPERIDOL SOLN 2MG/ML | PHARMASCIENCE INC | Solution | HALOPERIDOL 2 MG | Cancelled Post Market |
| 00552429 | RATIO-HALOPERIDOL 2MG/ML | RATIOPHARM INC DIVISION OF TEVA CANADA LIMITED | Solution | HALOPERIDOL 2 MG | Cancelled Post Market |
| 00728306 | RATIO-HALOPERIDOL TAB 10MG | RATIOPHARM INC DIVISION OF TEVA CANADA LIMITED | Tablet | HALOPERIDOL 10 MG | Cancelled Post Market |
| 00552143 | RATIO-HALOPERIDOL TAB 1MG | RATIOPHARM INC DIVISION OF TEVA CANADA LIMITED | Tablet | HALOPERIDOL 1 MG | Cancelled Post Market |
| 00728292 | RATIO-HALOPERIDOL TAB 2MG | RATIOPHARM INC DIVISION OF TEVA CANADA LIMITED | Tablet | HALOPERIDOL 2 MG | Cancelled Post Market |
| 00647969 | RATIO-HALOPERIDOL TAB 5MG | RATIOPHARM INC DIVISION OF TEVA CANADA LIMITED | Tablet | HALOPERIDOL 5 MG | Cancelled Post Market |
| 00768820 | TEVA-HALOPERIDOL | TEVA CANADA LIMITED | Tablet | HALOPERIDOL 20 MG | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 18485 | 2016-09-12 | Supplement to a New Drug Submission (SNDS) | CHANGE IN PRODUCT NAME; UPDATES TO THE PRODUCT MONOGTAPH AND LABELS |
| 15544 | 2014-04-25 | New Drug Submission (NDS) | MANUFACTURER NAME CHANGE |
International API supply for HALOPERIDOL
5 valid EDQM Certificates of Suitability from 5 holders. 13 active FDA Drug Master Files.
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